Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 91937 |
| ensemblid | ENSG00000145850.9 |
| hgncid | 25132 |
| symbol | TIMD4 |
| name | T cell immunoglobulin and mucin domain containing 4 |
| refseq_nuc | NM_138379.3 |
| refseq_prot | NP_612388.2 |
| ensembl_nuc | ENST00000274532.7 |
| ensembl_prot | ENSP00000274532.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 156919292 |
| end | 156963226 |
| strand | - |
| ver | v1.2 |
| region | chr5:156919292-156963226 |
| region5000 | chr5:156914292-156968226 |
| regionname0 | TIMD4_chr5_156919292_156963226 |
| regionname5000 | TIMD4_chr5_156914292_156968226 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 378 | 289 | 73 | 60 | 112 | 16 | 27 | 78 | TIMD4_chr5_156914292_156968226 | TIMD4 | MSKEP others(373): Show |
chr5 | 156914292 | 156968226 |
| a0002 | 0/0 | 378 | 7 | 4 | 3 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | MSKEP others(373): Show |
chr5 | 156914292 | 156968226 |
| a0003 | 0/0 | 378 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | MSKEP others(373): Show |
chr5 | 156914292 | 156968226 |
| a0004 | 1/0 | 378 | 4 | 0 | 3 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | MSKEP others(373): Show |
chr5 | 156914292 | 156968226 |
| a0005 | 0/0 | 378 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | MSKEP others(373): Show |
chr5 | 156914292 | 156968226 |
| a0006 | 0/0 | 378 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | MSKEP others(373): Show |
chr5 | 156914292 | 156968226 |
| a0007 | 0/0 | 378 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | MSKEP others(373): Show |
chr5 | 156914292 | 156968226 |
| a0008 | 0/0 | 378 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | MSKEP others(373): Show |
chr5 | 156914292 | 156968226 |
| a0009 | 0/0 | 378 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | MSKEP others(373): Show |
chr5 | 156914292 | 156968226 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1134 | 274 | 70 | 59 | 103 | 16 | 25 | TIMD4_chr5_156914292_156968226 | TIMD4 | ATGTC others(1129): Show |
chr5 | 156914292 | 156968226 | ||
| a0001c0002 | 0/0 | 1134 | 11 | 1 | 1 | 7 | 0 | 2 | TIMD4_chr5_156914292_156968226 | TIMD4 | ATGTC others(1129): Show |
chr5 | 156914292 | 156968226 | ||
| a0001c0007 | 0/0 | 1134 | 2 | 0 | 0 | 2 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | ATGTC others(1129): Show |
chr5 | 156914292 | 156968226 | ||
| a0001c0008 | 0/0 | 1134 | 2 | 2 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | ATGTC others(1129): Show |
chr5 | 156914292 | 156968226 | ||
| a0002c0003 | 0/0 | 1134 | 6 | 3 | 3 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | ATGTC others(1129): Show |
chr5 | 156914292 | 156968226 | ||
| a0002c0010 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | ATGTC others(1129): Show |
chr5 | 156914292 | 156968226 | ||
| a0003c0004 | 0/0 | 1134 | 6 | 6 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | ATGTC others(1129): Show |
chr5 | 156914292 | 156968226 | ||
| a0004c0005 | 1/0 | 1134 | 4 | 0 | 3 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | ATGTC others(1129): Show |
chr5 | 156914292 | 156968226 | ||
| a0005c0006 | 0/0 | 1134 | 2 | 2 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | ATGTC others(1129): Show |
chr5 | 156914292 | 156968226 | ||
| a0006c0013 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | ATGTC others(1129): Show |
chr5 | 156914292 | 156968226 | ||
| a0007c0012 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | ATGTC others(1129): Show |
chr5 | 156914292 | 156968226 | ||
| a0008c0011 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | ATGTC others(1129): Show |
chr5 | 156914292 | 156968226 | ||
| a0009c0009 | 0/0 | 1134 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | ATGTC others(1129): Show |
chr5 | 156914292 | 156968226 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1330 | 234 | 47 | 57 | 89 | 16 | 24 | TIMD4_chr5_156914292_156968226 | TIMD4 | AGACT others(1325): Show |
chr5 | 156914292 | 156968226 |
| a0001c0001t0002 | 0/0 | 1330 | 26 | 9 | 2 | 14 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | AGACT others(1325): Show |
chr5 | 156914292 | 156968226 |
| a0001c0001t0003 | 0/0 | 1329 | 14 | 14 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | AGACT others(1324): Show |
chr5 | 156914292 | 156968226 |
| a0001c0002t0001 | 0/0 | 1330 | 11 | 1 | 1 | 7 | 0 | 2 | TIMD4_chr5_156914292_156968226 | TIMD4 | AGACT others(1325): Show |
chr5 | 156914292 | 156968226 |
| a0001c0007t0001 | 0/0 | 1330 | 2 | 0 | 0 | 2 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | AGACT others(1325): Show |
chr5 | 156914292 | 156968226 |
| a0001c0008t0001 | 0/0 | 1330 | 2 | 2 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | AGACT others(1325): Show |
chr5 | 156914292 | 156968226 |
| a0002c0003t0001 | 0/0 | 1330 | 6 | 3 | 3 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | AGACT others(1325): Show |
chr5 | 156914292 | 156968226 |
| a0002c0010t0001 | 0/0 | 1330 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | AGACT others(1325): Show |
chr5 | 156914292 | 156968226 |
| a0003c0004t0001 | 0/0 | 1330 | 6 | 6 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | AGACT others(1325): Show |
chr5 | 156914292 | 156968226 |
| a0004c0005t0001 | 1/0 | 1330 | 4 | 0 | 3 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | AGACT others(1325): Show |
chr5 | 156914292 | 156968226 |
| a0005c0006t0001 | 0/0 | 1330 | 2 | 2 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | AGACT others(1325): Show |
chr5 | 156914292 | 156968226 |
| a0006c0013t0001 | 0/0 | 1330 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | AGACT others(1325): Show |
chr5 | 156914292 | 156968226 |
| a0007c0012t0001 | 0/0 | 1330 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | AGACT others(1325): Show |
chr5 | 156914292 | 156968226 |
| a0008c0011t0001 | 0/0 | 1330 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | AGACT others(1325): Show |
chr5 | 156914292 | 156968226 |
| a0009c0009t0001 | 0/0 | 1330 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | AGACT others(1325): Show |
chr5 | 156914292 | 156968226 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0168 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0007t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0007t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0008t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0001c0008t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0002c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0002c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0002c0003t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0002c0003t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0002c0003t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0002c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0002c0010t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0003c0004t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0003c0004t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0003c0004t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0003c0004t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0003c0004t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0004c0005t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0004c0005t0001g0248 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0004c0005t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0005c0006t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0005c0006t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0006c0013t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0007c0012t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0008c0011t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| a0009c0009t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | GBR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | GBR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | GBR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0245 | EUR | FIN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | CHS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | CHS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | CHS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | CHS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01070 | hp2 | a0002 | c0003 | t0001 | g0230 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01167 | hp2 | a0002 | c0003 | t0001 | g0231 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01169 | hp2 | a0002 | c0003 | t0001 | g0232 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01255 | hp1 | a0004 | c0005 | t0001 | g0249 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01257 | hp2 | a0004 | c0005 | t0001 | g0019 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01258 | hp1 | a0004 | c0005 | t0001 | g0019 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0049 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | IBS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | IBS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | IBS | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01884 | hp1 | a0006 | c0013 | t0001 | g0152 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01891 | hp2 | a0002 | c0003 | t0001 | g0045 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CDX | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CDX | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02451 | hp1 | a0003 | c0004 | t0001 | g0004 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02717 | hp2 | a0007 | c0012 | t0001 | g0069 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0233 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02723 | hp2 | a0002 | c0010 | t0001 | g0236 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02976 | hp2 | a0002 | c0003 | t0001 | g0121 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03195 | hp1 | a0008 | c0011 | t0001 | g0027 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03225 | hp1 | a0003 | c0004 | t0001 | g0004 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0051 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | GWD | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03579 | hp1 | a0003 | c0004 | t0001 | g0029 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0266 | SAS | PJL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0055 | SAS | BEB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG04204 | hp1 | a0009 | c0009 | t0001 | g0050 | SAS | STU | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | STU | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | STU | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18522 | hp1 | a0001 | c0008 | t0001 | g0158 | AFR | YRI | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | YRI | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | YRI | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | YRI | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18945 | hp1 | a0001 | c0007 | t0001 | g0133 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | LWK | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19062 | hp2 | a0001 | c0007 | t0001 | g0134 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | YRI | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA19240 | hp2 | a0003 | c0004 | t0001 | g0030 | AFR | YRI | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA20129 | hp1 | a0001 | c0008 | t0001 | g0229 | AFR | ASW | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ASW | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | TSI | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0244 | EUR | TSI | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | TSI | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | TSI | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | GIH | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | GIH | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02109 | hp2 | a0005 | c0006 | t0001 | g0234 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0278 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG02559 | hp2 | a0003 | c0004 | t0001 | g0028 | AFR | ACB | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03471 | hp1 | a0005 | c0006 | t0001 | g0269 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | USA | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| HG06807 | hp2 | a0003 | c0004 | t0001 | g0031 | AFR | USA | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | USA | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | USA | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0168 | REF | REF | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| homoSapiens | grch38p0 | a0004 | c0005 | t0001 | g0248 | REF | REF | TIMD4_chr5_156914292_156968226 | TIMD4 | chr5 | 156914292 | 156968226 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:156919501 | C | T | 2 | a0007 a0008 |
2 | HG02717.hp2 HG03195.hp1 |
missense_variant | MODERATE | c.1093G>A | p.Val365Met | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 9/9 | 1121/1330 | 1093/1137 | 365/378 | chr5 | 156919501 | |||
| chr5:156949692 | A | G | 8 | a0001 a0002 a0003 others(5): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
missense_variant | MODERATE | c.719T>C | p.Val240Ala | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 4/9 | 747/1330 | 719/1137 | 240/378 | chr5 | 156949692 | |||
| chr5:156951575 | G | T | 1 | a0009 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.616C>A | p.Pro206Thr | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/9 | 644/1330 | 616/1137 | 206/378 | chr5 | 156951575 | |||
| chr5:156951655 | G | A | 2 | a0003 a0008 |
7 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(4): Show |
missense_variant | MODERATE | c.536C>T | p.Thr179Ile | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/9 | 564/1330 | 536/1137 | 179/378 | chr5 | 156951655 | |||
| chr5:156951677 | C | T | 1 | a0005 | 2 | HG02109.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.514G>A | p.Val172Met | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/9 | 542/1330 | 514/1137 | 172/378 | chr5 | 156951677 | |||
| chr5:156951682 | G | T | 4 | a0002 a0003 a0006 others(1): Show |
15 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
missense_variant | MODERATE | c.509C>A | p.Thr170Lys | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/9 | 537/1330 | 509/1137 | 170/378 | chr5 | 156951682 | |||
| chr5:156954543 | G | A | 1 | a0006 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.272C>T | p.Pro91Leu | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/9 | 300/1330 | 272/1137 | 91/378 | chr5 | 156954543 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:156919499 | C | G | 1 | a0001c0007 | 2 | NA18945.hp1 NA19062.hp2 |
synonymous_variant | LOW | c.1095G>C | p.Val365Val | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 9/9 | 1123/1330 | 1095/1137 | 365/378 | chr5 | 156919499 | |||
| chr5:156919517 | T | C | 2 | a0001c0008 a0002c0010 |
3 | HG02723.hp2 NA18522.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.1077A>G | p.Lys359Lys | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 9/9 | 1105/1330 | 1077/1137 | 359/378 | chr5 | 156919517 | |||
| chr5:156954620 | C | T | 2 | a0001c0002 a0009c0009 |
12 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(9): Show |
synonymous_variant | LOW | c.195G>A | p.Lys65Lys | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/9 | 223/1330 | 195/1137 | 65/378 | chr5 | 156954620 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:156919423 | GC | G | 1 | a0001c0001t0003 | 14 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*33delG | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 9/9 | 33 | chr5 | 156919423 | ||||||
| chr5:156919453 | G | A | 1 | a0001c0001t0002 | 26 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 9/9 | 4 | chr5 | 156919453 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:156919830 | C | T | 23 | a0001c0001t0001g0048 a0001c0001t0001g0065 a0001c0001t0001g0066 others(20): Show |
26 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1053-289G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 8/8 | chr5 | 156919830 | |||||||
| chr5:156919895 | G | A | 12 | a0001c0001t0001g0048 a0001c0001t0001g0065 a0001c0001t0001g0066 others(9): Show |
12 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1053-354C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 8/8 | chr5 | 156919895 | |||||||
| chr5:156920171 | C | G | 12 | a0001c0001t0001g0048 a0001c0001t0001g0065 a0001c0001t0001g0066 others(9): Show |
12 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1052+293G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 8/8 | chr5 | 156920171 | |||||||
| chr5:156920203 | C | T | 28 | a0001c0001t0001g0014 a0001c0001t0001g0082 a0001c0001t0001g0108 others(25): Show |
29 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1052+261G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 8/8 | chr5 | 156920203 | |||||||
| chr5:156920261 | C | T | 3 | a0001c0008t0001g0158 a0001c0008t0001g0229 a0002c0010t0001g0236 |
3 | HG02723.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1052+203G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 8/8 | chr5 | 156920261 | |||||||
| chr5:156920267 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1052+197A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 8/8 | chr5 | 156920267 | |||||||
| chr5:156920341 | C | T | 10 | a0001c0001t0003g0001 a0001c0001t0003g0036 a0001c0001t0003g0037 others(7): Show |
13 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1052+123G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 8/8 | chr5 | 156920341 | |||||||
| chr5:156920541 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1013-38G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156920541 | |||||||
| chr5:156920701 | A | G | 24 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0032 others(21): Show |
26 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1013-198T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156920701 | |||||||
| chr5:156920805 | C | G | 3 | a0001c0008t0001g0158 a0001c0008t0001g0229 a0002c0010t0001g0236 |
3 | HG02723.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1013-302G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156920805 | |||||||
| chr5:156920846 | G | A | 1 | a0001c0001t0003g0037 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1013-343C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156920846 | |||||||
| chr5:156920908 | G | A | 51 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(48): Show |
55 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.1013-405C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156920908 | |||||||
| chr5:156921054 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1013-551G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921054 | |||||||
| chr5:156921198 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1013-695A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921198 | |||||||
| chr5:156921282 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1013-779C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921282 | |||||||
| chr5:156921551 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1012+548G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921551 | |||||||
| chr5:156921616 | C | CA | 19 | a0001c0001t0001g0026 a0001c0001t0001g0070 a0001c0001t0001g0077 others(16): Show |
19 | HG01346.hp2 HG01891.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.1012+482dupT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921616 | |||||||
| chr5:156921616 | CA | C | 11 | a0001c0001t0001g0064 a0001c0001t0001g0105 a0001c0001t0001g0126 others(8): Show |
11 | HG00558.hp1 HG01069.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.1012+482delT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921616 | |||||||
| chr5:156921616 | CAAA | C | 15 | a0001c0001t0002g0034 a0001c0001t0002g0237 a0001c0001t0002g0238 others(12): Show |
15 | HG01069.hp2 HG01071.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1012+480_1012+482d others(5): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921616 | |||||||
| chr5:156921616 | CAAAA | C | 13 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(10): Show |
14 | HG00597.hp2 HG01243.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1012+479_1012+482d others(6): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921616 | |||||||
| chr5:156921616 | CAAAAA | C | 14 | a0001c0001t0001g0015 a0001c0001t0001g0176 a0001c0001t0001g0180 others(11): Show |
18 | HG01978.hp2 HG02004.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1012+478_1012+482d others(7): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921616 | |||||||
| chr5:156921616 | CAAAAAA | C | 60 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0025 others(57): Show |
63 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1012+477_1012+482d others(8): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921616 | |||||||
| chr5:156921616 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1012+473_1012+482d others(12): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921616 | |||||||
| chr5:156921617 | A | C | 2 | a0001c0008t0001g0158 a0002c0010t0001g0236 |
2 | HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1012+482T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921617 | |||||||
| chr5:156921618 | A | C | 1 | a0001c0008t0001g0229 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1012+481T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921618 | |||||||
| chr5:156921644 | A | G | 2 | a0001c0008t0001g0158 a0002c0010t0001g0236 |
2 | HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1012+455T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921644 | |||||||
| chr5:156921706 | G | C | 1 | a0001c0001t0001g0196 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1012+393C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156921706 | |||||||
| chr5:156922066 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1012+33C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 7/8 | chr5 | 156922066 | |||||||
| chr5:156922351 | T | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(84): Show |
94 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.895-135A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156922351 | |||||||
| chr5:156922390 | C | T | 4 | a0001c0001t0001g0140 a0001c0001t0002g0005 a0001c0001t0002g0032 others(1): Show |
5 | HG03130.hp1 HG03453.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-174G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156922390 | |||||||
| chr5:156922650 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.895-434T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156922650 | |||||||
| chr5:156922652 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.895-436G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156922652 | |||||||
| chr5:156922780 | AGAGAT | A | 86 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(83): Show |
93 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.895-569_895-565del others(5): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156922780 | |||||||
| chr5:156922862 | G | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(109): Show |
121 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(118): Show |
intron_variant | MODIFIER | c.895-646C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156922862 | |||||||
| chr5:156922984 | T | A | 1 | a0001c0001t0001g0218 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.895-768A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156922984 | |||||||
| chr5:156923036 | A | T | 1 | a0001c0001t0001g0193 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.895-820T>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923036 | |||||||
| chr5:156923049 | A | G | 3 | a0001c0008t0001g0158 a0001c0008t0001g0229 a0002c0010t0001g0236 |
3 | HG02723.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.895-833T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923049 | |||||||
| chr5:156923090 | G | A | 5 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(2): Show |
5 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-874C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923090 | |||||||
| chr5:156923096 | C | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(44): Show |
51 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.895-880G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923096 | |||||||
| chr5:156923143 | A | AT | 8 | a0001c0001t0001g0002 a0001c0001t0001g0128 a0001c0001t0001g0129 others(5): Show |
8 | HG02572.hp1 HG03471.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.895-928dupA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923143 | |||||||
| chr5:156923143 | ATTTTT | A | 33 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0258 others(30): Show |
34 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.895-932_895-928del others(5): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923143 | |||||||
| chr5:156923143 | ATTTTTT | A | 76 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(73): Show |
83 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.895-933_895-928del others(6): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923143 | |||||||
| chr5:156923256 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.895-1040G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923256 | |||||||
| chr5:156923309 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.895-1093G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923309 | |||||||
| chr5:156923438 | T | A | 4 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.895-1222A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923438 | |||||||
| chr5:156923449 | TA | T | 61 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(58): Show |
65 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.895-1234delT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923449 | |||||||
| chr5:156923539 | A | AT | 27 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0032 others(24): Show |
29 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.895-1324dupA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923539 | |||||||
| chr5:156923580 | C | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(83): Show |
93 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.895-1364G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923580 | |||||||
| chr5:156923704 | AT | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(50): Show |
57 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.895-1489delA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923704 | |||||||
| chr5:156923739 | T | G | 9 | a0001c0001t0001g0043 a0001c0001t0001g0076 a0001c0001t0001g0077 others(6): Show |
9 | HG02451.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.895-1523A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923739 | |||||||
| chr5:156923797 | C | T | 4 | a0001c0001t0001g0090 a0001c0001t0001g0116 a0001c0001t0001g0117 others(1): Show |
4 | HG00099.hp2 HG00639.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.895-1581G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156923797 | |||||||
| chr5:156924020 | T | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(83): Show |
93 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.895-1804A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924020 | |||||||
| chr5:156924028 | G | C | 2 | a0007c0012t0001g0069 a0008c0011t0001g0027 |
2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.895-1812C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924028 | |||||||
| chr5:156924035 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.895-1819G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924035 | |||||||
| chr5:156924246 | C | T | 3 | a0001c0008t0001g0158 a0001c0008t0001g0229 a0002c0010t0001g0236 |
3 | HG02723.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.894+2017G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924246 | |||||||
| chr5:156924254 | T | C | 4 | a0001c0001t0002g0237 a0001c0001t0002g0238 a0001c0001t0002g0256 others(1): Show |
4 | HG02055.hp1 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+2009A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924254 | |||||||
| chr5:156924336 | T | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(68): Show |
78 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.894+1927A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924336 | |||||||
| chr5:156924375 | C | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0219 |
2 | NA18961.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.894+1888G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924375 | |||||||
| chr5:156924492 | G | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(83): Show |
93 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.894+1771C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924492 | |||||||
| chr5:156924635 | A | C | 4 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+1628T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924635 | |||||||
| chr5:156924663 | G | A | 86 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(83): Show |
93 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.894+1600C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924663 | |||||||
| chr5:156924665 | G | A | 1 | a0001c0001t0002g0238 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.894+1598C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156924665 | |||||||
| chr5:156925225 | G | A | 86 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(83): Show |
93 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.894+1038C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156925225 | |||||||
| chr5:156925267 | A | G | 89 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(86): Show |
96 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(93): Show |
intron_variant | MODIFIER | c.894+996T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156925267 | |||||||
| chr5:156925369 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0179 |
2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.894+894G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156925369 | |||||||
| chr5:156925575 | C | T | 4 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+688G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156925575 | |||||||
| chr5:156925742 | G | T | 2 | a0001c0001t0002g0237 a0001c0001t0002g0238 |
2 | HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.894+521C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156925742 | |||||||
| chr5:156925766 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.894+497C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156925766 | |||||||
| chr5:156925951 | T | C | 5 | a0001c0001t0001g0082 a0001c0001t0001g0157 a0001c0001t0001g0165 others(2): Show |
5 | HG02698.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.894+312A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156925951 | |||||||
| chr5:156926058 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.894+205G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156926058 | |||||||
| chr5:156926170 | C | G | 1 | a0001c0001t0002g0255 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.894+93G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 6/8 | chr5 | 156926170 | |||||||
| chr5:156926397 | T | A | 4 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.845-85A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156926397 | |||||||
| chr5:156926434 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.845-122G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156926434 | |||||||
| chr5:156926677 | T | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0217 |
2 | NA18945.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.845-365A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156926677 | |||||||
| chr5:156926686 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.845-374G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156926686 | |||||||
| chr5:156926725 | A | G | 52 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(49): Show |
56 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.845-413T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156926725 | |||||||
| chr5:156926892 | T | C | 4 | a0001c0001t0002g0237 a0001c0001t0002g0238 a0001c0001t0002g0256 others(1): Show |
4 | HG02055.hp1 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.845-580A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156926892 | |||||||
| chr5:156927003 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.845-691G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927003 | |||||||
| chr5:156927089 | T | A | 2 | a0005c0006t0001g0234 a0005c0006t0001g0269 |
2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.845-777A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927089 | |||||||
| chr5:156927133 | C | T | 10 | a0001c0001t0003g0001 a0001c0001t0003g0036 a0001c0001t0003g0037 others(7): Show |
13 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.845-821G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927133 | |||||||
| chr5:156927163 | G | T | 3 | a0001c0001t0002g0005 a0001c0001t0002g0032 a0001c0001t0002g0034 |
4 | HG03130.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.845-851C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927163 | |||||||
| chr5:156927184 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.845-872T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927184 | |||||||
| chr5:156927272 | T | A | 6 | a0001c0001t0001g0235 a0001c0001t0001g0258 a0002c0003t0001g0230 others(3): Show |
6 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.845-960A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927272 | |||||||
| chr5:156927297 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.845-985T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927297 | |||||||
| chr5:156927409 | C | T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG00140.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.845-1097G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927409 | |||||||
| chr5:156927466 | G | A | 103 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(100): Show |
109 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.845-1154C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927466 | |||||||
| chr5:156927591 | G | A | 2 | a0001c0001t0003g0042 a0001c0001t0003g0044 |
2 | HG02615.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.845-1279C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927591 | |||||||
| chr5:156927708 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.845-1396A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927708 | |||||||
| chr5:156927888 | A | C | 1 | a0001c0001t0001g0272 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.845-1576T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156927888 | |||||||
| chr5:156928140 | C | A | 113 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(110): Show |
122 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(119): Show |
intron_variant | MODIFIER | c.845-1828G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928140 | |||||||
| chr5:156928157 | G | C | 2 | a0001c0001t0001g0209 a0001c0001t0001g0226 |
2 | HG00741.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.845-1845C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928157 | |||||||
| chr5:156928170 | C | T | 24 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0032 others(21): Show |
26 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.845-1858G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928170 | |||||||
| chr5:156928246 | C | A | 20 | a0001c0001t0002g0020 a0001c0001t0002g0035 a0001c0001t0002g0237 others(17): Show |
21 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.845-1934G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928246 | |||||||
| chr5:156928295 | T | TA | 14 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0073 others(11): Show |
18 | HG00558.hp2 HG02027.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.845-1984dupT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928295 | |||||||
| chr5:156928295 | T | TAA | 63 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(60): Show |
67 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.845-1985_845-1984d others(4): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928295 | |||||||
| chr5:156928352 | A | G | 20 | a0001c0001t0002g0020 a0001c0001t0002g0035 a0001c0001t0002g0237 others(17): Show |
21 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.845-2040T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928352 | |||||||
| chr5:156928364 | A | G | 113 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(110): Show |
122 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(119): Show |
intron_variant | MODIFIER | c.845-2052T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928364 | |||||||
| chr5:156928391 | G | T | 6 | a0001c0001t0001g0235 a0002c0003t0001g0121 a0002c0003t0001g0230 others(3): Show |
6 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.845-2079C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928391 | |||||||
| chr5:156928459 | C | T | 23 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0032 others(20): Show |
25 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.845-2147G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928459 | |||||||
| chr5:156928490 | G | A | 4 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.845-2178C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928490 | |||||||
| chr5:156928663 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.845-2351T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928663 | |||||||
| chr5:156928710 | T | C | 1 | a0001c0001t0001g0008 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.845-2398A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928710 | |||||||
| chr5:156928794 | T | C | 1 | a0001c0001t0003g0037 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.845-2482A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928794 | |||||||
| chr5:156928949 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.845-2637C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156928949 | |||||||
| chr5:156929038 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.845-2726A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156929038 | |||||||
| chr5:156929283 | T | C | 16 | a0001c0001t0002g0020 a0001c0001t0002g0035 a0001c0001t0002g0250 others(13): Show |
17 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.845-2971A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156929283 | |||||||
| chr5:156929295 | C | A | 2 | a0001c0001t0002g0274 a0001c0001t0002g0275 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.845-2983G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156929295 | |||||||
| chr5:156929338 | G | A | 2 | a0005c0006t0001g0234 a0005c0006t0001g0269 |
2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.845-3026C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156929338 | |||||||
| chr5:156929467 | A | G | 70 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(67): Show |
74 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.845-3155T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156929467 | |||||||
| chr5:156929566 | CGA | C | 10 | a0001c0001t0003g0001 a0001c0001t0003g0036 a0001c0001t0003g0037 others(7): Show |
13 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.845-3256_845-3255d others(4): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156929566 | |||||||
| chr5:156929723 | A | G | 1 | a0001c0002t0001g0056 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.845-3411T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156929723 | |||||||
| chr5:156929806 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.845-3494G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156929806 | |||||||
| chr5:156929897 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0080 |
2 | HG02683.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.845-3585G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156929897 | |||||||
| chr5:156929962 | T | C | 1 | a0001c0001t0002g0034 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.845-3650A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156929962 | |||||||
| chr5:156930005 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0059 a0001c0001t0001g0061 |
4 | HG01099.hp1 HG03491.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.845-3693G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930005 | |||||||
| chr5:156930018 | T | C | 4 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.845-3706A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930018 | |||||||
| chr5:156930059 | C | G | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.845-3747G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930059 | |||||||
| chr5:156930074 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.845-3762C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930074 | |||||||
| chr5:156930127 | A | G | 64 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(61): Show |
68 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.845-3815T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930127 | |||||||
| chr5:156930133 | T | C | 10 | a0001c0001t0003g0001 a0001c0001t0003g0036 a0001c0001t0003g0037 others(7): Show |
13 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.845-3821A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930133 | |||||||
| chr5:156930146 | G | T | 12 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0048 others(9): Show |
12 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.845-3834C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930146 | |||||||
| chr5:156930150 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.845-3838G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930150 | |||||||
| chr5:156930159 | G | T | 3 | a0001c0008t0001g0158 a0001c0008t0001g0229 a0002c0010t0001g0236 |
3 | HG02723.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.845-3847C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930159 | |||||||
| chr5:156930425 | T | C | 10 | a0001c0001t0003g0001 a0001c0001t0003g0036 a0001c0001t0003g0037 others(7): Show |
13 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.845-4113A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930425 | |||||||
| chr5:156930451 | A | T | 2 | a0007c0012t0001g0069 a0008c0011t0001g0027 |
2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.845-4139T>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930451 | |||||||
| chr5:156930587 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.845-4275T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930587 | |||||||
| chr5:156930863 | T | C | 6 | a0001c0001t0001g0235 a0002c0003t0001g0121 a0002c0003t0001g0230 others(3): Show |
6 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.845-4551A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156930863 | |||||||
| chr5:156931008 | G | T | 5 | a0003c0004t0001g0004 a0003c0004t0001g0028 a0003c0004t0001g0029 others(2): Show |
6 | HG02451.hp1 HG02559.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.845-4696C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156931008 | |||||||
| chr5:156931452 | T | C | 1 | a0001c0001t0003g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.845-5140A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156931452 | |||||||
| chr5:156931659 | A | G | 2 | a0007c0012t0001g0069 a0008c0011t0001g0027 |
2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.845-5347T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156931659 | |||||||
| chr5:156931842 | G | C | 16 | a0001c0001t0002g0020 a0001c0001t0002g0035 a0001c0001t0002g0250 others(13): Show |
17 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.845-5530C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156931842 | |||||||
| chr5:156931843 | C | A | 16 | a0001c0001t0002g0020 a0001c0001t0002g0035 a0001c0001t0002g0250 others(13): Show |
17 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.845-5531G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156931843 | |||||||
| chr5:156931845 | AAGATACT others(164): Show |
A | 16 | a0001c0001t0002g0020 a0001c0001t0002g0035 a0001c0001t0002g0250 others(13): Show |
17 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.845-5704_845-5534d others(2): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156931845 | |||||||
| chr5:156932018 | CT | C | 16 | a0001c0001t0002g0020 a0001c0001t0002g0035 a0001c0001t0002g0250 others(13): Show |
17 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.845-5707delA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932018 | |||||||
| chr5:156932020 | T | C | 16 | a0001c0001t0002g0020 a0001c0001t0002g0035 a0001c0001t0002g0250 others(13): Show |
17 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.845-5708A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932020 | |||||||
| chr5:156932026 | A | T | 16 | a0001c0001t0002g0020 a0001c0001t0002g0035 a0001c0001t0002g0250 others(13): Show |
17 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.845-5714T>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932026 | |||||||
| chr5:156932028 | G | C | 16 | a0001c0001t0002g0020 a0001c0001t0002g0035 a0001c0001t0002g0250 others(13): Show |
17 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.845-5716C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932028 | |||||||
| chr5:156932029 | G | A | 16 | a0001c0001t0002g0020 a0001c0001t0002g0035 a0001c0001t0002g0250 others(13): Show |
17 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.845-5717C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932029 | |||||||
| chr5:156932030 | A | T | 16 | a0001c0001t0002g0020 a0001c0001t0002g0035 a0001c0001t0002g0250 others(13): Show |
17 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.845-5718T>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932030 | |||||||
| chr5:156932038 | T | C | 3 | a0001c0008t0001g0158 a0001c0008t0001g0229 a0002c0010t0001g0236 |
3 | HG02723.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.845-5726A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932038 | |||||||
| chr5:156932072 | T | C | 4 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.845-5760A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932072 | |||||||
| chr5:156932081 | T | C | 12 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0048 others(9): Show |
12 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.845-5769A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932081 | |||||||
| chr5:156932264 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.845-5952A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932264 | |||||||
| chr5:156932283 | T | G | 3 | a0001c0001t0002g0005 a0001c0001t0002g0032 a0001c0001t0002g0034 |
4 | HG03130.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.845-5971A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932283 | |||||||
| chr5:156932391 | A | G | 20 | a0001c0001t0002g0020 a0001c0001t0002g0035 a0001c0001t0002g0237 others(17): Show |
21 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.845-6079T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932391 | |||||||
| chr5:156932424 | A | G | 1 | a0001c0001t0001g0218 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.845-6112T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932424 | |||||||
| chr5:156932469 | C | G | 2 | a0007c0012t0001g0069 a0008c0011t0001g0027 |
2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.845-6157G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932469 | |||||||
| chr5:156932488 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.845-6176C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932488 | |||||||
| chr5:156932531 | C | T | 3 | a0001c0008t0001g0158 a0001c0008t0001g0229 a0002c0010t0001g0236 |
3 | HG02723.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.845-6219G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932531 | |||||||
| chr5:156932717 | G | A | 23 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0032 others(20): Show |
25 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.845-6405C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932717 | |||||||
| chr5:156932754 | C | A | 13 | a0001c0001t0002g0020 a0001c0001t0002g0250 a0001c0001t0002g0251 others(10): Show |
14 | HG00597.hp2 HG03704.hp2 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.845-6442G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932754 | |||||||
| chr5:156932784 | A | G | 3 | a0001c0008t0001g0158 a0001c0008t0001g0229 a0002c0010t0001g0236 |
3 | HG02723.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.845-6472T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932784 | |||||||
| chr5:156932866 | T | G | 1 | a0001c0001t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.845-6554A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932866 | |||||||
| chr5:156932897 | C | A | 4 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.845-6585G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156932897 | |||||||
| chr5:156933003 | C | CAA | 23 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0032 others(20): Show |
25 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.845-6693_845-6692d others(4): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933003 | |||||||
| chr5:156933006 | A | AAAAAG | 49 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(46): Show |
53 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.845-6699_845-6695d others(7): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933006 | |||||||
| chr5:156933006 | A | AAAAAGAA others(3): Show |
2 | a0001c0001t0001g0209 a0001c0001t0001g0281 |
2 | HG00741.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.845-6704_845-6695d others(12): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933006 | |||||||
| chr5:156933006 | A | AAAAAGAA others(8): Show |
6 | a0001c0001t0001g0025 a0001c0001t0001g0203 a0001c0001t0001g0272 others(3): Show |
6 | HG02055.hp2 HG02735.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.845-6709_845-6695d others(17): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933006 | |||||||
| chr5:156933006 | A | AAAAAGAA others(13): Show |
2 | a0001c0001t0001g0110 a0001c0001t0001g0271 |
2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.845-6714_845-6695d others(22): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933006 | |||||||
| chr5:156933006 | A | AAAAAGAA others(18): Show |
3 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0280 |
3 | HG02922.hp2 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.845-6719_845-6695d others(27): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933006 | |||||||
| chr5:156933006 | A | AAAAAGAA others(38): Show |
1 | a0005c0006t0001g0269 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.845-6695_845-6694i others(47): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933006 | |||||||
| chr5:156933006 | A | AAAAAGAA others(43): Show |
1 | a0005c0006t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.845-6695_845-6694i others(52): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933006 | |||||||
| chr5:156933144 | T | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0075 a0001c0001t0001g0079 others(2): Show |
6 | HG00558.hp2 HG02056.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.845-6832A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933144 | |||||||
| chr5:156933172 | G | C | 110 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(107): Show |
118 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.845-6860C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933172 | |||||||
| chr5:156933182 | A | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(84): Show |
93 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.845-6870T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933182 | |||||||
| chr5:156933211 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.845-6899C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933211 | |||||||
| chr5:156933263 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0139 |
2 | NA18942.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.845-6951A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933263 | |||||||
| chr5:156933297 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.845-6985C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933297 | |||||||
| chr5:156933338 | A | G | 52 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(49): Show |
56 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.845-7026T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933338 | |||||||
| chr5:156933371 | A | G | 10 | a0001c0001t0003g0001 a0001c0001t0003g0036 a0001c0001t0003g0037 others(7): Show |
13 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.845-7059T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933371 | |||||||
| chr5:156933440 | T | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(103): Show |
115 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.845-7128A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933440 | |||||||
| chr5:156933457 | A | AC | 16 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0046 others(13): Show |
16 | HG02027.hp1 HG02027.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.845-7146dupG | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933457 | |||||||
| chr5:156933544 | G | GTTGTT | 56 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(53): Show |
60 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.845-7237_845-7233d others(7): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933544 | |||||||
| chr5:156933544 | G | GTTGTTTT others(3): Show |
16 | a0001c0001t0001g0033 a0001c0001t0001g0082 a0001c0001t0001g0173 others(13): Show |
16 | HG01928.hp1 HG02055.hp2 HG02698.hp1 others(13): Show |
intron_variant | MODIFIER | c.845-7242_845-7233d others(12): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933544 | |||||||
| chr5:156933544 | G | GTTGTTTT others(8): Show |
13 | a0001c0001t0002g0020 a0001c0001t0002g0250 a0001c0001t0002g0252 others(10): Show |
14 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.845-7247_845-7233d others(17): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933544 | |||||||
| chr5:156933544 | G | GTTGTTTT others(13): Show |
4 | a0001c0001t0002g0005 a0001c0001t0002g0032 a0001c0001t0002g0034 others(1): Show |
5 | HG03130.hp1 HG03453.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.845-7252_845-7233d others(22): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933544 | |||||||
| chr5:156933544 | GTTGTT | G | 173 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(170): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.845-7237_845-7233d others(7): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933544 | |||||||
| chr5:156933544 | GTTGTTTT others(3): Show |
G | 2 | a0001c0001t0001g0149 a0001c0001t0001g0217 |
2 | NA18945.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.845-7242_845-7233d others(12): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933544 | |||||||
| chr5:156933606 | C | A | 2 | a0001c0001t0002g0250 a0001c0001t0002g0254 |
2 | NA18941.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.845-7294G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933606 | |||||||
| chr5:156933716 | G | A | 1 | a0007c0012t0001g0069 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.845-7404C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933716 | |||||||
| chr5:156933805 | C | A | 7 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(4): Show |
7 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.845-7493G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933805 | |||||||
| chr5:156933893 | C | T | 4 | a0001c0001t0001g0154 a0001c0001t0001g0163 a0001c0001t0001g0201 others(1): Show |
4 | HG00735.hp2 HG01256.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.845-7581G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933893 | |||||||
| chr5:156933942 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.845-7630T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156933942 | |||||||
| chr5:156934129 | C | T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0114 |
3 | HG02630.hp2 HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.845-7817G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934129 | |||||||
| chr5:156934152 | CT | C | 8 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0271 others(5): Show |
8 | HG02055.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.845-7841delA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934152 | |||||||
| chr5:156934246 | T | G | 1 | a0001c0001t0001g0239 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.845-7934A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934246 | |||||||
| chr5:156934288 | T | TA | 3 | a0001c0001t0002g0005 a0001c0001t0002g0032 a0001c0001t0002g0034 |
4 | HG03130.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.845-7977dupT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934288 | |||||||
| chr5:156934315 | G | T | 1 | a0001c0007t0001g0133 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.845-8003C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934315 | |||||||
| chr5:156934431 | G | A | 10 | a0001c0001t0003g0001 a0001c0001t0003g0036 a0001c0001t0003g0037 others(7): Show |
13 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.845-8119C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934431 | |||||||
| chr5:156934431 | G | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(5): Show |
10 | HG01261.hp1 HG01516.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.845-8119C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934431 | |||||||
| chr5:156934440 | G | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0110 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.845-8128C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934440 | |||||||
| chr5:156934529 | T | C | 2 | a0007c0012t0001g0069 a0008c0011t0001g0027 |
2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.845-8217A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934529 | |||||||
| chr5:156934541 | G | C | 113 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(110): Show |
122 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(119): Show |
intron_variant | MODIFIER | c.845-8229C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934541 | |||||||
| chr5:156934564 | T | A | 1 | a0001c0001t0001g0101 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.845-8252A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934564 | |||||||
| chr5:156934665 | G | T | 1 | a0001c0001t0001g0247 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.845-8353C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934665 | |||||||
| chr5:156934705 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.845-8393A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934705 | |||||||
| chr5:156934773 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.845-8461G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156934773 | |||||||
| chr5:156935006 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0059 a0001c0001t0001g0061 |
4 | HG01099.hp1 HG03491.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.845-8694T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156935006 | |||||||
| chr5:156935031 | C | A | 1 | a0001c0001t0002g0264 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.845-8719G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156935031 | |||||||
| chr5:156935062 | C | T | 1 | a0001c0001t0002g0263 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.845-8750G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156935062 | |||||||
| chr5:156935070 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.845-8758A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156935070 | |||||||
| chr5:156935135 | T | C | 4 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.845-8823A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156935135 | |||||||
| chr5:156935182 | C | CT | 20 | a0001c0001t0002g0020 a0001c0001t0002g0035 a0001c0001t0002g0237 others(17): Show |
21 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.845-8871dupA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156935182 | |||||||
| chr5:156935473 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.845-9161G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156935473 | |||||||
| chr5:156935713 | C | A | 1 | a0001c0001t0001g0075 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.845-9401G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156935713 | |||||||
| chr5:156936040 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.845-9728T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936040 | |||||||
| chr5:156936067 | C | T | 10 | a0001c0001t0003g0001 a0001c0001t0003g0036 a0001c0001t0003g0037 others(7): Show |
13 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.845-9755G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936067 | |||||||
| chr5:156936119 | G | A | 3 | a0001c0008t0001g0158 a0001c0008t0001g0229 a0002c0010t0001g0236 |
3 | HG02723.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.845-9807C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936119 | |||||||
| chr5:156936141 | C | A | 2 | a0007c0012t0001g0069 a0008c0011t0001g0027 |
2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.845-9829G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936141 | |||||||
| chr5:156936142 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.845-9830C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936142 | |||||||
| chr5:156936153 | C | T | 89 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(86): Show |
95 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.845-9841G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936153 | |||||||
| chr5:156936173 | A | G | 2 | a0001c0001t0002g0253 a0001c0001t0002g0265 |
2 | NA19005.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.845-9861T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936173 | |||||||
| chr5:156936216 | G | A | 8 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0271 others(5): Show |
8 | HG02055.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.845-9904C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936216 | |||||||
| chr5:156936622 | T | C | 4 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.845-10310A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936622 | |||||||
| chr5:156936800 | C | T | 1 | a0005c0006t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.845-10488G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936800 | |||||||
| chr5:156936919 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.845-10607C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936919 | |||||||
| chr5:156936932 | G | GA | 49 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0048 others(46): Show |
54 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.845-10621dupT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156936932 | |||||||
| chr5:156937027 | C | T | 2 | a0005c0006t0001g0234 a0005c0006t0001g0269 |
2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.845-10715G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156937027 | |||||||
| chr5:156937028 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.845-10716C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156937028 | |||||||
| chr5:156937192 | C | T | 1 | a0001c0001t0001g0008 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.845-10880G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156937192 | |||||||
| chr5:156937196 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.845-10884C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156937196 | |||||||
| chr5:156937382 | C | CAG | 56 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(53): Show |
60 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.844+11032_844+1103 others(6): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156937382 | |||||||
| chr5:156937437 | G | T | 8 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0271 others(5): Show |
8 | HG02055.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.844+10979C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156937437 | |||||||
| chr5:156937465 | C | G | 2 | a0001c0008t0001g0158 a0002c0010t0001g0236 |
2 | HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.844+10951G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156937465 | |||||||
| chr5:156937477 | C | T | 1 | a0009c0009t0001g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.844+10939G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156937477 | |||||||
| chr5:156937586 | A | AC | 6 | a0001c0001t0001g0235 a0002c0003t0001g0121 a0002c0003t0001g0230 others(3): Show |
6 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.844+10829dupG | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156937586 | |||||||
| chr5:156937998 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.844+10418G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156937998 | |||||||
| chr5:156938044 | T | C | 4 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.844+10372A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156938044 | |||||||
| chr5:156938239 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.844+10177G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156938239 | |||||||
| chr5:156938355 | T | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(84): Show |
93 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.844+10061A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156938355 | |||||||
| chr5:156938461 | A | C | 89 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(86): Show |
95 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.844+9955T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156938461 | |||||||
| chr5:156938565 | G | A | 89 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(86): Show |
95 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.844+9851C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156938565 | |||||||
| chr5:156938669 | G | A | 5 | a0001c0001t0001g0033 a0001c0001t0001g0280 a0001c0001t0002g0005 others(2): Show |
6 | HG02965.hp2 HG03130.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.844+9747C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156938669 | |||||||
| chr5:156938725 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0217 |
2 | NA18945.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.844+9691C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156938725 | |||||||
| chr5:156938836 | C | T | 9 | a0001c0001t0003g0001 a0001c0001t0003g0036 a0001c0001t0003g0037 others(6): Show |
12 | HG01884.hp2 HG02615.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.844+9580G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156938836 | |||||||
| chr5:156938912 | G | A | 10 | a0001c0001t0003g0001 a0001c0001t0003g0036 a0001c0001t0003g0037 others(7): Show |
13 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.844+9504C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156938912 | |||||||
| chr5:156939094 | C | A | 1 | a0001c0001t0001g0143 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.844+9322G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156939094 | |||||||
| chr5:156939170 | G | A | 89 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(86): Show |
95 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.844+9246C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156939170 | |||||||
| chr5:156939285 | T | C | 89 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(86): Show |
95 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.844+9131A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156939285 | |||||||
| chr5:156939355 | G | A | 8 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0271 others(5): Show |
8 | HG02055.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.844+9061C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156939355 | |||||||
| chr5:156939448 | G | T | 1 | a0001c0002t0001g0055 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.844+8968C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156939448 | |||||||
| chr5:156939677 | T | C | 10 | a0001c0001t0003g0001 a0001c0001t0003g0036 a0001c0001t0003g0037 others(7): Show |
13 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.844+8739A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156939677 | |||||||
| chr5:156939775 | G | A | 13 | a0001c0001t0002g0253 a0001c0001t0003g0001 a0001c0001t0003g0036 others(10): Show |
16 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.844+8641C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156939775 | |||||||
| chr5:156939977 | G | A | 2 | a0001c0008t0001g0158 a0002c0010t0001g0236 |
2 | HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.844+8439C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156939977 | |||||||
| chr5:156940081 | T | C | 227 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(224): Show |
245 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.844+8335A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940081 | |||||||
| chr5:156940189 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0210 |
2 | NA18960.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.844+8227G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940189 | |||||||
| chr5:156940204 | C | T | 4 | a0001c0001t0001g0258 a0001c0008t0001g0158 a0001c0008t0001g0229 others(1): Show |
4 | HG02723.hp2 NA18522.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.844+8212G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940204 | |||||||
| chr5:156940246 | A | G | 89 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(86): Show |
95 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.844+8170T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940246 | |||||||
| chr5:156940289 | G | A | 51 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(48): Show |
55 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.844+8127C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940289 | |||||||
| chr5:156940317 | T | A | 1 | a0001c0002t0001g0054 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.844+8099A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940317 | |||||||
| chr5:156940324 | C | T | 14 | a0001c0001t0001g0048 a0001c0001t0001g0110 a0001c0001t0003g0001 others(11): Show |
17 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.844+8092G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940324 | |||||||
| chr5:156940369 | G | T | 1 | a0001c0001t0001g0210 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.844+8047C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940369 | |||||||
| chr5:156940399 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.844+8017C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940399 | |||||||
| chr5:156940419 | C | G | 4 | a0001c0001t0001g0048 a0001c0001t0001g0110 a0005c0006t0001g0234 others(1): Show |
4 | HG02109.hp2 HG02257.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.844+7997G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940419 | |||||||
| chr5:156940447 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.844+7969G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940447 | |||||||
| chr5:156940475 | G | A | 3 | a0001c0001t0002g0005 a0001c0001t0002g0032 a0001c0001t0002g0034 |
4 | HG03130.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.844+7941C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940475 | |||||||
| chr5:156940515 | A | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(92): Show |
101 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.844+7901T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940515 | |||||||
| chr5:156940528 | C | T | 28 | a0001c0001t0001g0014 a0001c0001t0001g0082 a0001c0001t0001g0108 others(25): Show |
29 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.844+7888G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940528 | |||||||
| chr5:156940573 | G | A | 1 | a0005c0006t0001g0269 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.844+7843C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940573 | |||||||
| chr5:156940592 | CCTCTGCC others(30): Show |
C | 12 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0048 others(9): Show |
12 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.844+7787_844+7823d others(39): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940592 | |||||||
| chr5:156940650 | A | G | 89 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(86): Show |
95 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.844+7766T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940650 | |||||||
| chr5:156940727 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0139 |
2 | NA18942.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.844+7689C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940727 | |||||||
| chr5:156940744 | A | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(85): Show |
94 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.844+7672T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940744 | |||||||
| chr5:156940792 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG02129.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.844+7624C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940792 | |||||||
| chr5:156940799 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.844+7617C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940799 | |||||||
| chr5:156940818 | C | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(83): Show |
92 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.844+7598G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156940818 | |||||||
| chr5:156941021 | G | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(102): Show |
114 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(111): Show |
intron_variant | MODIFIER | c.844+7395C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156941021 | |||||||
| chr5:156941040 | T | A | 6 | a0001c0001t0001g0109 a0001c0001t0001g0160 a0001c0001t0001g0161 others(3): Show |
6 | HG01081.hp2 HG01361.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.844+7376A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156941040 | |||||||
| chr5:156941051 | A | C | 19 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0048 others(16): Show |
20 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.844+7365T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156941051 | |||||||
| chr5:156941093 | T | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG00558.hp1 HG02135.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.844+7323A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156941093 | |||||||
| chr5:156941185 | C | T | 2 | a0007c0012t0001g0069 a0008c0011t0001g0027 |
2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.844+7231G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156941185 | |||||||
| chr5:156941186 | G | A | 17 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0048 others(14): Show |
18 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.844+7230C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156941186 | |||||||
| chr5:156942052 | G | A | 13 | a0001c0001t0002g0005 a0001c0001t0002g0032 a0001c0001t0002g0034 others(10): Show |
17 | HG01884.hp2 HG02615.hp1 HG02818.hp1 others(14): Show |
intron_variant | MODIFIER | c.844+6364C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942052 | |||||||
| chr5:156942138 | G | A | 2 | a0002c0003t0001g0045 a0006c0013t0001g0152 |
2 | HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.844+6278C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942138 | |||||||
| chr5:156942160 | C | T | 231 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(228): Show |
249 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.844+6256G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942160 | |||||||
| chr5:156942175 | C | T | 12 | a0001c0001t0001g0235 a0001c0001t0001g0258 a0001c0002t0001g0006 others(9): Show |
14 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.844+6241G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942175 | |||||||
| chr5:156942205 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.844+6211A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942205 | |||||||
| chr5:156942287 | C | T | 2 | a0007c0012t0001g0069 a0008c0011t0001g0027 |
2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.844+6129G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942287 | |||||||
| chr5:156942359 | T | C | 10 | a0001c0001t0001g0048 a0001c0008t0001g0229 a0002c0003t0001g0045 others(7): Show |
10 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.844+6057A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942359 | |||||||
| chr5:156942463 | C | T | 10 | a0001c0001t0001g0048 a0001c0008t0001g0229 a0002c0003t0001g0045 others(7): Show |
10 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.844+5953G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942463 | |||||||
| chr5:156942657 | C | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0179 a0001c0008t0001g0158 |
3 | HG02886.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.844+5759G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942657 | |||||||
| chr5:156942658 | C | T | 2 | a0001c0001t0001g0008 a0001c0008t0001g0229 |
3 | HG01256.hp1 HG01258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.844+5758G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942658 | |||||||
| chr5:156942748 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.844+5668A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942748 | |||||||
| chr5:156942761 | T | C | 2 | a0007c0012t0001g0069 a0008c0011t0001g0027 |
2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.844+5655A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942761 | |||||||
| chr5:156942985 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.844+5431A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156942985 | |||||||
| chr5:156943018 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.844+5398A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943018 | |||||||
| chr5:156943057 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0227 |
2 | HG01099.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.844+5359G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943057 | |||||||
| chr5:156943162 | C | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0129 |
2 | NA18985.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.844+5254G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943162 | |||||||
| chr5:156943240 | T | C | 4 | a0002c0003t0001g0230 a0002c0003t0001g0231 a0002c0003t0001g0232 others(1): Show |
4 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.844+5176A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943240 | |||||||
| chr5:156943298 | G | T | 1 | a0001c0008t0001g0229 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.844+5118C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943298 | |||||||
| chr5:156943362 | G | A | 3 | a0002c0003t0001g0045 a0002c0003t0001g0121 a0006c0013t0001g0152 |
3 | HG01884.hp1 HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.844+5054C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943362 | |||||||
| chr5:156943393 | T | C | 10 | a0001c0001t0001g0048 a0001c0008t0001g0229 a0002c0003t0001g0045 others(7): Show |
10 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.844+5023A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943393 | |||||||
| chr5:156943555 | T | A | 1 | a0001c0001t0001g0148 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.844+4861A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943555 | |||||||
| chr5:156943558 | G | C | 10 | a0001c0001t0001g0048 a0001c0008t0001g0229 a0002c0003t0001g0045 others(7): Show |
10 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.844+4858C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943558 | |||||||
| chr5:156943602 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.844+4814T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943602 | |||||||
| chr5:156943653 | T | G | 1 | a0001c0001t0001g0137 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.844+4763A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943653 | |||||||
| chr5:156943663 | T | A | 1 | a0001c0001t0001g0181 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.844+4753A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943663 | |||||||
| chr5:156943818 | A | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(266): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.844+4598T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943818 | |||||||
| chr5:156943878 | C | T | 1 | a0001c0008t0001g0229 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.844+4538G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943878 | |||||||
| chr5:156943879 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.844+4537C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943879 | |||||||
| chr5:156943895 | C | CA | 19 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0086 others(16): Show |
20 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.844+4520dupT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943895 | |||||||
| chr5:156943895 | CA | C | 13 | a0001c0001t0001g0057 a0001c0001t0002g0020 a0001c0001t0002g0250 others(10): Show |
14 | HG00597.hp2 HG01884.hp1 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.844+4520delT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943895 | |||||||
| chr5:156943987 | G | A | 10 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0049 others(7): Show |
12 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.844+4429C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156943987 | |||||||
| chr5:156944073 | AG | A | 7 | a0001c0001t0001g0048 a0001c0008t0001g0229 a0002c0003t0001g0230 others(4): Show |
7 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.844+4342delC | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944073 | |||||||
| chr5:156944483 | C | T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG00140.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.844+3933G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944483 | |||||||
| chr5:156944495 | C | CT | 42 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0061 others(39): Show |
43 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.844+3920dupA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944495 | |||||||
| chr5:156944495 | C | CTT | 8 | a0001c0001t0001g0010 a0001c0001t0001g0086 a0001c0001t0001g0270 others(5): Show |
9 | HG01071.hp2 HG02055.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.844+3919_844+3920d others(4): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944495 | |||||||
| chr5:156944495 | CT | C | 140 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(137): Show |
153 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.844+3920delA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944495 | |||||||
| chr5:156944495 | CTT | C | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0002g0268 others(3): Show |
6 | HG01884.hp1 HG01891.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.844+3919_844+3920d others(4): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944495 | |||||||
| chr5:156944495 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0221 |
2 | HG01891.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.844+3909_844+3920d others(14): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944495 | |||||||
| chr5:156944502 | T | C | 3 | a0002c0003t0001g0045 a0002c0003t0001g0121 a0006c0013t0001g0152 |
3 | HG01884.hp1 HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.844+3914A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944502 | |||||||
| chr5:156944727 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.844+3689C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944727 | |||||||
| chr5:156944740 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.844+3676G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944740 | |||||||
| chr5:156944747 | C | T | 8 | a0002c0003t0001g0045 a0002c0003t0001g0121 a0002c0003t0001g0230 others(5): Show |
8 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.844+3669G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944747 | |||||||
| chr5:156944817 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.844+3599C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944817 | |||||||
| chr5:156944820 | A | C | 1 | a0001c0001t0001g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.844+3596T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944820 | |||||||
| chr5:156944874 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.844+3542G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944874 | |||||||
| chr5:156944881 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.844+3535A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156944881 | |||||||
| chr5:156945126 | T | A | 2 | a0005c0006t0001g0234 a0005c0006t0001g0269 |
2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.844+3290A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156945126 | |||||||
| chr5:156945233 | A | G | 1 | a0001c0001t0001g0008 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.844+3183T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156945233 | |||||||
| chr5:156945448 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.844+2968C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156945448 | |||||||
| chr5:156945573 | A | G | 11 | a0001c0001t0001g0048 a0001c0001t0001g0110 a0001c0008t0001g0229 others(8): Show |
11 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.844+2843T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156945573 | |||||||
| chr5:156945648 | T | C | 1 | a0002c0010t0001g0236 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.844+2768A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156945648 | |||||||
| chr5:156945671 | A | G | 3 | a0001c0001t0001g0283 a0005c0006t0001g0234 a0005c0006t0001g0269 |
3 | HG02109.hp2 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.844+2745T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156945671 | |||||||
| chr5:156945767 | T | G | 1 | a0001c0001t0001g0177 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.844+2649A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156945767 | |||||||
| chr5:156945932 | C | T | 1 | a0001c0002t0001g0049 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.844+2484G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156945932 | |||||||
| chr5:156946256 | T | C | 1 | a0005c0006t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.844+2160A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946256 | |||||||
| chr5:156946373 | G | A | 3 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0259 |
3 | HG02258.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.844+2043C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946373 | |||||||
| chr5:156946406 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.844+2010A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946406 | |||||||
| chr5:156946422 | T | G | 1 | a0002c0010t0001g0236 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.844+1994A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946422 | |||||||
| chr5:156946479 | T | G | 1 | a0001c0001t0001g0281 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.844+1937A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946479 | |||||||
| chr5:156946513 | G | T | 10 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0049 others(7): Show |
12 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.844+1903C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946513 | |||||||
| chr5:156946578 | G | A | 17 | a0001c0001t0001g0025 a0001c0001t0001g0270 a0001c0001t0001g0271 others(14): Show |
17 | HG01069.hp2 HG01071.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.844+1838C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946578 | |||||||
| chr5:156946602 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.844+1814C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946602 | |||||||
| chr5:156946625 | C | T | 4 | a0002c0003t0001g0230 a0002c0003t0001g0231 a0002c0003t0001g0232 others(1): Show |
4 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.844+1791G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946625 | |||||||
| chr5:156946626 | G | C | 188 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(185): Show |
199 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.844+1790C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946626 | |||||||
| chr5:156946649 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.844+1767A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946649 | |||||||
| chr5:156946653 | A | AT | 7 | a0001c0001t0001g0141 a0003c0004t0001g0004 a0003c0004t0001g0028 others(4): Show |
8 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.844+1762dupA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946653 | |||||||
| chr5:156946775 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.844+1641C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946775 | |||||||
| chr5:156946964 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.844+1452C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156946964 | |||||||
| chr5:156947003 | A | C | 17 | a0001c0001t0001g0048 a0001c0001t0001g0110 a0001c0008t0001g0229 others(14): Show |
18 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.844+1413T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156947003 | |||||||
| chr5:156947156 | C | A | 8 | a0002c0003t0001g0045 a0002c0003t0001g0121 a0002c0003t0001g0230 others(5): Show |
8 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.844+1260G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156947156 | |||||||
| chr5:156947197 | C | CA | 13 | a0001c0001t0001g0108 a0001c0001t0001g0127 a0001c0001t0001g0155 others(10): Show |
13 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.844+1218dupT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156947197 | |||||||
| chr5:156947213 | T | C | 3 | a0002c0003t0001g0045 a0002c0003t0001g0121 a0006c0013t0001g0152 |
3 | HG01884.hp1 HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.844+1203A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156947213 | |||||||
| chr5:156947213 | TAGAA | T | 6 | a0003c0004t0001g0004 a0003c0004t0001g0028 a0003c0004t0001g0029 others(3): Show |
7 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.844+1199_844+1202d others(6): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156947213 | |||||||
| chr5:156947478 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.844+938T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156947478 | |||||||
| chr5:156947513 | A | G | 1 | a0001c0001t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.844+903T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156947513 | |||||||
| chr5:156947639 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0261 |
2 | HG02015.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.844+777G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156947639 | |||||||
| chr5:156947670 | A | G | 1 | a0001c0001t0002g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.844+746T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156947670 | |||||||
| chr5:156947683 | C | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0110 a0001c0008t0001g0229 |
3 | HG02257.hp1 HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.844+733G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156947683 | |||||||
| chr5:156948324 | C | CAA | 11 | a0001c0001t0001g0048 a0001c0001t0001g0110 a0001c0008t0001g0229 others(8): Show |
11 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.844+90_844+91dupTT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156948324 | |||||||
| chr5:156948324 | CA | C | 7 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0094 others(4): Show |
7 | HG01346.hp2 HG02056.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.844+91delT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156948324 | |||||||
| chr5:156948361 | T | A | 30 | a0001c0001t0001g0014 a0001c0001t0001g0108 a0001c0001t0001g0154 others(27): Show |
31 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.844+55A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 5/8 | chr5 | 156948361 | |||||||
| chr5:156949209 | G | T | 1 | a0001c0001t0001g0140 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.760+442C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 4/8 | chr5 | 156949209 | |||||||
| chr5:156949265 | C | T | 11 | a0001c0001t0001g0048 a0001c0001t0001g0110 a0001c0008t0001g0229 others(8): Show |
11 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.760+386G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 4/8 | chr5 | 156949265 | |||||||
| chr5:156949367 | G | C | 1 | a0001c0001t0002g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.760+284C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 4/8 | chr5 | 156949367 | |||||||
| chr5:156949418 | C | CCCT | 7 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0072 others(4): Show |
10 | HG01516.hp1 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.760+230_760+232dup others(3): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 4/8 | chr5 | 156949418 | |||||||
| chr5:156949418 | CCCT | C | 166 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(163): Show |
175 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.760+230_760+232del others(3): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 4/8 | chr5 | 156949418 | |||||||
| chr5:156949418 | CCCTCCT | C | 33 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0016 others(30): Show |
38 | HG00423.hp2 HG01261.hp1 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.760+227_760+232del others(6): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 4/8 | chr5 | 156949418 | |||||||
| chr5:156949418 | CCCTCCTC others(2): Show |
C | 13 | a0001c0001t0001g0279 a0001c0001t0001g0282 a0001c0001t0001g0283 others(10): Show |
13 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.760+224_760+232del others(9): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 4/8 | chr5 | 156949418 | |||||||
| chr5:156949429 | C | T | 1 | a0002c0010t0001g0236 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.760+222G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 4/8 | chr5 | 156949429 | |||||||
| chr5:156949638 | A | G | 1 | a0001c0001t0002g0251 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.760+13T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 4/8 | chr5 | 156949638 | |||||||
| chr5:156949811 | T | A | 6 | a0003c0004t0001g0004 a0003c0004t0001g0028 a0003c0004t0001g0029 others(3): Show |
7 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.680-80A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156949811 | |||||||
| chr5:156949863 | G | T | 16 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(13): Show |
16 | HG01069.hp2 HG01071.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.680-132C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156949863 | |||||||
| chr5:156949883 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.680-152A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156949883 | |||||||
| chr5:156950060 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.680-329G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156950060 | |||||||
| chr5:156950119 | CT | C | 208 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(205): Show |
220 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.680-389delA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156950119 | |||||||
| chr5:156950215 | G | C | 17 | a0001c0001t0001g0048 a0001c0001t0001g0110 a0001c0008t0001g0229 others(14): Show |
18 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.680-484C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156950215 | |||||||
| chr5:156950275 | T | C | 3 | a0001c0001t0001g0060 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG00140.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.680-544A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156950275 | |||||||
| chr5:156950341 | C | T | 16 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(13): Show |
16 | HG01069.hp2 HG01071.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.680-610G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156950341 | |||||||
| chr5:156950471 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.680-740A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156950471 | |||||||
| chr5:156950762 | G | A | 16 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(13): Show |
16 | HG01069.hp2 HG01071.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.679+750C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156950762 | |||||||
| chr5:156950832 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.679+680C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156950832 | |||||||
| chr5:156950848 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.679+664C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156950848 | |||||||
| chr5:156950855 | C | T | 1 | a0001c0008t0001g0158 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.679+657G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156950855 | |||||||
| chr5:156951004 | T | TCTA | 5 | a0003c0004t0001g0004 a0003c0004t0001g0028 a0003c0004t0001g0029 others(2): Show |
6 | HG02451.hp1 HG02559.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.679+507_679+508ins others(3): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951004 | |||||||
| chr5:156951006 | G | A | 5 | a0003c0004t0001g0004 a0003c0004t0001g0028 a0003c0004t0001g0029 others(2): Show |
6 | HG02451.hp1 HG02559.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.679+506C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951006 | |||||||
| chr5:156951007 | T | C | 5 | a0003c0004t0001g0004 a0003c0004t0001g0028 a0003c0004t0001g0029 others(2): Show |
6 | HG02451.hp1 HG02559.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.679+505A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951007 | |||||||
| chr5:156951007 | T | TAC | 152 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(149): Show |
161 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.679+503_679+504dup others(2): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951007 | |||||||
| chr5:156951007 | T | TACAC | 11 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(8): Show |
11 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.679+501_679+504dup others(4): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951007 | |||||||
| chr5:156951007 | T | TACACACA others(1): Show |
3 | a0001c0001t0001g0110 a0001c0008t0001g0229 a0002c0010t0001g0236 |
3 | HG02257.hp1 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.679+497_679+504dup others(8): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951007 | |||||||
| chr5:156951007 | T | TACACACA others(3): Show |
3 | a0002c0003t0001g0230 a0002c0003t0001g0231 a0002c0003t0001g0233 |
3 | HG01070.hp2 HG01167.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.679+495_679+504dup others(10): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951007 | |||||||
| chr5:156951007 | T | TACACACA others(5): Show |
1 | a0002c0003t0001g0232 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.679+493_679+504dup others(12): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951007 | |||||||
| chr5:156951031 | C | A | 1 | a0001c0001t0001g0273 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.679+481G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951031 | |||||||
| chr5:156951038 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.679+474G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951038 | |||||||
| chr5:156951067 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.679+445G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951067 | |||||||
| chr5:156951119 | A | G | 17 | a0001c0001t0001g0048 a0001c0001t0001g0110 a0001c0008t0001g0229 others(14): Show |
18 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.679+393T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951119 | |||||||
| chr5:156951131 | C | A | 10 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0049 others(7): Show |
12 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.679+381G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951131 | |||||||
| chr5:156951272 | A | G | 1 | a0002c0010t0001g0236 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.679+240T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 3/8 | chr5 | 156951272 | |||||||
| chr5:156951939 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.401-149A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156951939 | |||||||
| chr5:156952019 | G | C | 3 | a0002c0003t0001g0045 a0002c0003t0001g0121 a0006c0013t0001g0152 |
3 | HG01884.hp1 HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.401-229C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952019 | |||||||
| chr5:156952042 | C | T | 8 | a0002c0003t0001g0045 a0002c0003t0001g0121 a0002c0003t0001g0230 others(5): Show |
8 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.401-252G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952042 | |||||||
| chr5:156952214 | T | C | 3 | a0001c0001t0001g0138 a0001c0001t0001g0150 a0001c0001t0001g0151 |
3 | NA18957.hp1 NA18974.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.401-424A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952214 | |||||||
| chr5:156952289 | C | CA | 18 | a0001c0001t0001g0199 a0001c0001t0001g0270 a0001c0001t0001g0271 others(15): Show |
19 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.401-500dupT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952289 | |||||||
| chr5:156952487 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.401-697G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952487 | |||||||
| chr5:156952511 | T | G | 1 | a0001c0001t0001g0092 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.401-721A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952511 | |||||||
| chr5:156952520 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.401-730T>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952520 | |||||||
| chr5:156952529 | G | A | 1 | a0002c0003t0001g0045 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.401-739C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952529 | |||||||
| chr5:156952537 | A | G | 8 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(5): Show |
8 | HG01069.hp2 HG01071.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.401-747T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952537 | |||||||
| chr5:156952669 | A | G | 1 | a0001c0001t0001g0191 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.401-879T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952669 | |||||||
| chr5:156952973 | ACCT | A | 10 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0049 others(7): Show |
12 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.401-1186_401-1184d others(5): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156952973 | |||||||
| chr5:156953030 | C | T | 2 | a0003c0004t0001g0028 a0003c0004t0001g0029 |
2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.401-1240G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953030 | |||||||
| chr5:156953056 | T | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(189): Show |
203 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.401-1266A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953056 | |||||||
| chr5:156953467 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0059 |
3 | HG01099.hp1 HG04204.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.400+948G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953467 | |||||||
| chr5:156953477 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.400+938C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953477 | |||||||
| chr5:156953579 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.400+836C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953579 | |||||||
| chr5:156953653 | C | CA | 70 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0043 others(67): Show |
77 | HG00408.hp2 HG00597.hp2 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.400+761dupT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953653 | |||||||
| chr5:156953653 | C | CAA | 141 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(138): Show |
150 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.400+760_400+761dup others(2): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953653 | |||||||
| chr5:156953653 | CAAAAAAA others(3): Show |
C | 6 | a0003c0004t0001g0004 a0003c0004t0001g0028 a0003c0004t0001g0029 others(3): Show |
7 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.400+752_400+761del others(10): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953653 | |||||||
| chr5:156953676 | G | A | 14 | a0001c0001t0001g0033 a0001c0001t0002g0005 a0001c0001t0002g0032 others(11): Show |
18 | HG01884.hp2 HG02615.hp1 HG02818.hp1 others(15): Show |
intron_variant | MODIFIER | c.400+739C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953676 | |||||||
| chr5:156953678 | G | A | 14 | a0001c0001t0001g0033 a0001c0001t0002g0005 a0001c0001t0002g0032 others(11): Show |
18 | HG01884.hp2 HG02615.hp1 HG02818.hp1 others(15): Show |
intron_variant | MODIFIER | c.400+737C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953678 | |||||||
| chr5:156953711 | T | A | 6 | a0001c0001t0001g0025 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
6 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.400+704A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953711 | |||||||
| chr5:156953766 | C | G | 6 | a0003c0004t0001g0004 a0003c0004t0001g0028 a0003c0004t0001g0029 others(3): Show |
7 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.400+649G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953766 | |||||||
| chr5:156953856 | G | A | 1 | a0006c0013t0001g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.400+559C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953856 | |||||||
| chr5:156953897 | G | A | 17 | a0001c0001t0001g0048 a0001c0001t0001g0110 a0001c0008t0001g0229 others(14): Show |
18 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.400+518C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156953897 | |||||||
| chr5:156954026 | C | A | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.400+389G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156954026 | |||||||
| chr5:156954030 | T | C | 17 | a0001c0001t0001g0048 a0001c0001t0001g0110 a0001c0008t0001g0229 others(14): Show |
18 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.400+385A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156954030 | |||||||
| chr5:156954057 | T | G | 6 | a0003c0004t0001g0004 a0003c0004t0001g0028 a0003c0004t0001g0029 others(3): Show |
7 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.400+358A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156954057 | |||||||
| chr5:156954163 | C | A | 1 | a0001c0001t0001g0078 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.400+252G>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156954163 | |||||||
| chr5:156954172 | AC | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0110 a0001c0008t0001g0229 |
3 | HG02257.hp1 HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.400+242delG | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156954172 | |||||||
| chr5:156954174 | G | A | 1 | a0001c0001t0001g0243 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.400+241C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156954174 | |||||||
| chr5:156954359 | G | A | 209 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(206): Show |
221 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.400+56C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 2/8 | chr5 | 156954359 | |||||||
| chr5:156954884 | C | CTT | 15 | a0001c0001t0001g0048 a0001c0001t0001g0110 a0001c0008t0001g0229 others(12): Show |
16 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-130_59-129dupAA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156954884 | |||||||
| chr5:156954884 | CT | C | 10 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0049 others(7): Show |
12 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-129delA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156954884 | |||||||
| chr5:156954921 | A | G | 1 | a0005c0006t0001g0269 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.59-165T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156954921 | |||||||
| chr5:156954986 | T | C | 15 | a0001c0001t0001g0048 a0001c0001t0001g0110 a0001c0008t0001g0229 others(12): Show |
16 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-230A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156954986 | |||||||
| chr5:156955024 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0202 |
2 | HG00735.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.59-268G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955024 | |||||||
| chr5:156955064 | C | G | 1 | a0001c0001t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.59-308G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955064 | |||||||
| chr5:156955202 | G | A | 2 | a0001c0001t0001g0176 a0002c0003t0001g0045 |
2 | HG01891.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.59-446C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955202 | |||||||
| chr5:156955297 | A | G | 163 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(160): Show |
172 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.59-541T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955297 | |||||||
| chr5:156955327 | G | A | 15 | a0001c0001t0001g0048 a0001c0001t0001g0110 a0001c0008t0001g0229 others(12): Show |
16 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-571C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955327 | |||||||
| chr5:156955431 | C | T | 1 | a0002c0003t0001g0045 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.59-675G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955431 | |||||||
| chr5:156955433 | G | A | 1 | a0002c0010t0001g0236 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.59-677C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955433 | |||||||
| chr5:156955528 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.59-772G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955528 | |||||||
| chr5:156955535 | G | A | 15 | a0001c0001t0001g0048 a0001c0001t0001g0110 a0001c0008t0001g0229 others(12): Show |
16 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-779C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955535 | |||||||
| chr5:156955564 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.59-808C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955564 | |||||||
| chr5:156955738 | C | T | 1 | a0001c0001t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.59-982G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955738 | |||||||
| chr5:156955879 | G | A | 10 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0049 others(7): Show |
12 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-1123C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156955879 | |||||||
| chr5:156956001 | G | A | 15 | a0001c0001t0001g0048 a0001c0001t0001g0110 a0001c0008t0001g0229 others(12): Show |
16 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-1245C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956001 | |||||||
| chr5:156956147 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.59-1391G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956147 | |||||||
| chr5:156956206 | T | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0216 |
2 | NA19062.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.59-1450A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956206 | |||||||
| chr5:156956254 | C | G | 10 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0049 others(7): Show |
12 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-1498G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956254 | |||||||
| chr5:156956281 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.59-1525G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956281 | |||||||
| chr5:156956411 | A | G | 193 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(190): Show |
204 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.59-1655T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956411 | |||||||
| chr5:156956442 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.59-1686C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956442 | |||||||
| chr5:156956526 | G | A | 1 | a0002c0010t0001g0236 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.59-1770C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956526 | |||||||
| chr5:156956724 | T | C | 2 | a0005c0006t0001g0234 a0005c0006t0001g0269 |
2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.59-1968A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956724 | |||||||
| chr5:156956882 | A | G | 1 | a0002c0003t0001g0045 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.59-2126T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956882 | |||||||
| chr5:156956918 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.59-2162G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156956918 | |||||||
| chr5:156957090 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.59-2334G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957090 | |||||||
| chr5:156957091 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.59-2335C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957091 | |||||||
| chr5:156957242 | A | G | 2 | a0001c0001t0001g0048 a0001c0008t0001g0229 |
2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.59-2486T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957242 | |||||||
| chr5:156957504 | G | C | 223 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(220): Show |
239 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.59-2748C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957504 | |||||||
| chr5:156957512 | C | CAAAAA | 12 | a0001c0001t0001g0048 a0002c0003t0001g0045 a0002c0003t0001g0231 others(9): Show |
13 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-2761_59-2757dup others(5): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957512 | |||||||
| chr5:156957512 | C | CAAAAAAA | 29 | a0001c0001t0001g0025 a0001c0001t0001g0235 a0001c0001t0001g0270 others(26): Show |
31 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.59-2763_59-2757dup others(7): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957512 | |||||||
| chr5:156957512 | C | CAAAAAAA others(1): Show |
29 | a0001c0001t0001g0026 a0001c0001t0001g0065 a0001c0001t0001g0066 others(26): Show |
30 | HG00597.hp2 HG01099.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.59-2764_59-2757dup others(8): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957512 | |||||||
| chr5:156957512 | C | CAAAAAAA others(2): Show |
140 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(137): Show |
151 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.59-2765_59-2757dup others(9): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957512 | |||||||
| chr5:156957512 | C | CAAAAAAA others(3): Show |
4 | a0001c0001t0001g0095 a0001c0001t0001g0170 a0001c0001t0001g0191 others(1): Show |
4 | HG02074.hp2 HG02738.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-2766_59-2757dup others(10): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957512 | |||||||
| chr5:156957613 | C | T | 4 | a0001c0001t0001g0279 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02572.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-2857G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957613 | |||||||
| chr5:156957706 | C | G | 1 | a0001c0001t0001g0171 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.59-2950G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957706 | |||||||
| chr5:156957767 | G | T | 1 | a0001c0001t0001g0261 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.59-3011C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957767 | |||||||
| chr5:156957942 | G | T | 4 | a0001c0001t0001g0131 a0001c0001t0001g0193 a0001c0007t0001g0133 others(1): Show |
4 | HG02080.hp2 NA18945.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3186C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957942 | |||||||
| chr5:156957995 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.59-3239G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156957995 | |||||||
| chr5:156958042 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.59-3286C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958042 | |||||||
| chr5:156958145 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0086 |
3 | HG02056.hp1 HG02135.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.59-3389C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958145 | |||||||
| chr5:156958145 | G | T | 1 | a0001c0008t0001g0229 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.59-3389C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958145 | |||||||
| chr5:156958170 | G | A | 15 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(12): Show |
15 | HG01069.hp2 HG01071.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.59-3414C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958170 | |||||||
| chr5:156958171 | C | T | 14 | a0001c0001t0001g0033 a0001c0001t0002g0005 a0001c0001t0002g0032 others(11): Show |
18 | HG01884.hp2 HG02615.hp1 HG02818.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-3415G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958171 | |||||||
| chr5:156958196 | C | T | 12 | a0002c0003t0001g0045 a0002c0003t0001g0230 a0002c0003t0001g0231 others(9): Show |
13 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-3440G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958196 | |||||||
| chr5:156958216 | T | G | 13 | a0001c0001t0002g0020 a0001c0001t0002g0250 a0001c0001t0002g0251 others(10): Show |
14 | HG00597.hp2 HG03704.hp2 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-3460A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958216 | |||||||
| chr5:156958305 | G | GAAGGA | 7 | a0001c0001t0001g0061 a0001c0001t0001g0261 a0001c0002t0001g0006 others(4): Show |
8 | HG01255.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3554_59-3550dup others(5): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | |||||||
| chr5:156958305 | G | GAAGGAAA others(3): Show |
7 | a0001c0001t0001g0182 a0001c0001t0001g0247 a0001c0001t0001g0262 others(4): Show |
9 | HG00408.hp2 HG00673.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-3559_59-3550dup others(10): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | |||||||
| chr5:156958305 | G | GAAGGAAA others(8): Show |
1 | a0001c0001t0001g0089 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.59-3564_59-3550dup others(15): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | |||||||
| chr5:156958305 | GAAGGA | G | 27 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0060 others(24): Show |
29 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.59-3554_59-3550del others(5): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | |||||||
| chr5:156958305 | GAAGGAAA others(3): Show |
G | 27 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0059 others(24): Show |
30 | HG00738.hp1 HG01069.hp1 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.59-3559_59-3550del others(10): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | |||||||
| chr5:156958305 | GAAGGAAA others(8): Show |
G | 28 | a0001c0001t0001g0015 a0001c0001t0001g0046 a0001c0001t0001g0047 others(25): Show |
29 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.59-3564_59-3550del others(15): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | |||||||
| chr5:156958305 | GAAGGAAA others(13): Show |
G | 38 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(35): Show |
42 | HG00735.hp2 HG00738.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.59-3569_59-3550del others(20): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | |||||||
| chr5:156958305 | GAAGGAAA others(18): Show |
G | 38 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0094 others(35): Show |
42 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.59-3574_59-3550del others(25): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | |||||||
| chr5:156958305 | GAAGGAAA others(23): Show |
G | 57 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(54): Show |
60 | HG00423.hp2 HG00558.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.59-3579_59-3550del others(30): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | |||||||
| chr5:156958305 | GAAGGAAA others(28): Show |
G | 10 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0033 others(7): Show |
11 | HG01074.hp1 HG01257.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-3584_59-3550del others(35): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | |||||||
| chr5:156958305 | GAAGGAAA others(33): Show |
G | 13 | a0001c0001t0001g0025 a0001c0001t0001g0065 a0001c0001t0001g0066 others(10): Show |
13 | HG00597.hp2 HG01243.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.59-3589_59-3550del others(40): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | |||||||
| chr5:156958305 | GAAGGAAA others(38): Show |
G | 16 | a0001c0001t0002g0020 a0001c0001t0002g0251 a0001c0001t0002g0252 others(13): Show |
18 | HG02451.hp1 HG02559.hp2 HG03225.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-3594_59-3550del others(45): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | |||||||
| chr5:156958305 | GAAGGAAA others(43): Show |
G | 3 | a0001c0001t0001g0129 a0001c0001t0002g0250 a0008c0011t0001g0027 |
3 | HG03195.hp1 NA18941.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.59-3599_59-3550del others(50): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958305 | |||||||
| chr5:156958313 | GGAAAGGA others(15): Show |
G | 1 | a0001c0001t0001g0210 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.59-3579_59-3558del others(22): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958313 | |||||||
| chr5:156958374 | G | T | 1 | a0001c0002t0001g0049 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.59-3618C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958374 | |||||||
| chr5:156958697 | C | T | 6 | a0003c0004t0001g0004 a0003c0004t0001g0028 a0003c0004t0001g0029 others(3): Show |
7 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3941G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958697 | |||||||
| chr5:156958796 | A | G | 2 | a0001c0001t0001g0048 a0001c0008t0001g0229 |
2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.59-4040T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958796 | |||||||
| chr5:156958821 | G | A | 4 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(1): Show |
4 | NA18957.hp2 NA19058.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-4065C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958821 | |||||||
| chr5:156958894 | T | C | 7 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG00099.hp2 HG00639.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-4138A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958894 | |||||||
| chr5:156958934 | A | G | 1 | a0001c0001t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.59-4178T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958934 | |||||||
| chr5:156958945 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.59-4189T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958945 | |||||||
| chr5:156958973 | TA | T | 14 | a0001c0001t0001g0048 a0001c0008t0001g0229 a0002c0003t0001g0045 others(11): Show |
15 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.58+4167delT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156958973 | |||||||
| chr5:156959159 | G | T | 1 | a0001c0001t0001g0129 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.58+3982C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959159 | |||||||
| chr5:156959440 | A | C | 2 | a0001c0001t0001g0048 a0001c0008t0001g0229 |
2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.58+3701T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959440 | |||||||
| chr5:156959563 | C | G | 14 | a0001c0001t0001g0048 a0001c0008t0001g0229 a0002c0003t0001g0045 others(11): Show |
15 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.58+3578G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959563 | |||||||
| chr5:156959630 | A | C | 1 | a0001c0001t0003g0278 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.58+3511T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959630 | |||||||
| chr5:156959653 | C | T | 3 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0219 |
3 | NA18961.hp2 NA18987.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.58+3488G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959653 | |||||||
| chr5:156959729 | A | T | 14 | a0001c0001t0001g0048 a0001c0008t0001g0229 a0002c0003t0001g0045 others(11): Show |
15 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.58+3412T>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959729 | |||||||
| chr5:156959877 | C | G | 15 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0002g0005 others(12): Show |
19 | HG01884.hp2 HG02451.hp2 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.58+3264G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959877 | |||||||
| chr5:156959906 | G | T | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.58+3235C>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959906 | |||||||
| chr5:156959911 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG02523.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.58+3230G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959911 | |||||||
| chr5:156959916 | G | A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0227 |
2 | HG01099.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.58+3225C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959916 | |||||||
| chr5:156959936 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.58+3205C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156959936 | |||||||
| chr5:156960096 | GA | G | 272 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(269): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.58+3044delT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960096 | |||||||
| chr5:156960096 | GAA | G | 10 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0049 others(7): Show |
12 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.58+3043_58+3044del others(2): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960096 | |||||||
| chr5:156960126 | G | C | 163 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(160): Show |
172 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.58+3015C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960126 | |||||||
| chr5:156960405 | C | CT | 20 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0033 others(17): Show |
22 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.58+2735dupA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960405 | |||||||
| chr5:156960405 | CT | C | 45 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0026 others(42): Show |
47 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.58+2735delA | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960405 | |||||||
| chr5:156960406 | T | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0216 |
2 | NA19062.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.58+2735A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960406 | |||||||
| chr5:156960409 | T | G | 1 | a0001c0001t0001g0183 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.58+2732A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960409 | |||||||
| chr5:156960411 | T | A | 1 | a0001c0001t0001g0183 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.58+2730A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960411 | |||||||
| chr5:156960412 | T | A | 1 | a0001c0001t0001g0183 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.58+2729A>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960412 | |||||||
| chr5:156960425 | C | G | 223 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(220): Show |
239 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.58+2716G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960425 | |||||||
| chr5:156960429 | A | C | 1 | a0001c0001t0001g0183 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.58+2712T>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960429 | |||||||
| chr5:156960443 | G | C | 1 | a0001c0001t0001g0183 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.58+2698C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960443 | |||||||
| chr5:156960444 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.58+2697A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960444 | |||||||
| chr5:156960463 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.58+2678C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960463 | |||||||
| chr5:156960617 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG00558.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.58+2524C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960617 | |||||||
| chr5:156960640 | C | T | 18 | a0001c0001t0001g0012 a0001c0001t0001g0096 a0001c0001t0001g0097 others(15): Show |
19 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.58+2501G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960640 | |||||||
| chr5:156960677 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.58+2464C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960677 | |||||||
| chr5:156960777 | A | G | 1 | a0002c0003t0001g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.58+2364T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960777 | |||||||
| chr5:156960795 | C | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0094 a0001c0001t0001g0095 others(3): Show |
6 | HG01346.hp2 HG02056.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.58+2346G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960795 | |||||||
| chr5:156960817 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.58+2324A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960817 | |||||||
| chr5:156960834 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.58+2307C>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960834 | |||||||
| chr5:156960869 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.58+2272T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960869 | |||||||
| chr5:156960892 | C | G | 13 | a0001c0001t0001g0235 a0001c0001t0001g0258 a0001c0001t0003g0278 others(10): Show |
15 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.58+2249G>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960892 | |||||||
| chr5:156960988 | G | A | 13 | a0001c0001t0002g0020 a0001c0001t0002g0250 a0001c0001t0002g0251 others(10): Show |
14 | HG00597.hp2 HG03704.hp2 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.58+2153C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156960988 | |||||||
| chr5:156961248 | G | A | 14 | a0001c0001t0001g0235 a0001c0001t0002g0256 a0001c0001t0002g0257 others(11): Show |
16 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.58+1893C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961248 | |||||||
| chr5:156961327 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.58+1814G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961327 | |||||||
| chr5:156961354 | A | G | 2 | a0005c0006t0001g0234 a0005c0006t0001g0269 |
2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.58+1787T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961354 | |||||||
| chr5:156961360 | T | G | 1 | a0005c0006t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.58+1781A>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961360 | |||||||
| chr5:156961451 | C | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
5 | HG00597.hp1 HG02071.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+1690G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961451 | |||||||
| chr5:156961512 | G | A | 2 | a0001c0001t0001g0235 a0001c0001t0003g0278 |
2 | HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.58+1629C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961512 | |||||||
| chr5:156961657 | G | GCCAGGCA others(21): Show |
15 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0002g0005 others(12): Show |
19 | HG01884.hp2 HG02451.hp2 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.58+1456_58+1483dup others(28): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961657 | |||||||
| chr5:156961702 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.58+1439G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961702 | |||||||
| chr5:156961720 | G | A | 6 | a0001c0001t0001g0184 a0003c0004t0001g0004 a0003c0004t0001g0028 others(3): Show |
7 | HG02451.hp1 HG02559.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+1421C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961720 | |||||||
| chr5:156961751 | C | T | 1 | a0002c0010t0001g0236 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.58+1390G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961751 | |||||||
| chr5:156961765 | T | C | 38 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0048 others(35): Show |
45 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.58+1376A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961765 | |||||||
| chr5:156961803 | C | T | 11 | a0001c0001t0001g0048 a0001c0002t0001g0006 a0001c0002t0001g0007 others(8): Show |
13 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+1338G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961803 | |||||||
| chr5:156961808 | C | CA | 39 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0094 others(36): Show |
40 | HG00099.hp2 HG00558.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.58+1332dupT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961808 | |||||||
| chr5:156961808 | C | CAA | 69 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(66): Show |
74 | HG00140.hp1 HG00408.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.58+1331_58+1332dup others(2): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961808 | |||||||
| chr5:156961808 | C | CAAA | 41 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0021 others(38): Show |
43 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.58+1330_58+1332dup others(3): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961808 | |||||||
| chr5:156961808 | C | CAAAA | 15 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0219 others(12): Show |
15 | HG01069.hp2 HG01071.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.58+1329_58+1332dup others(4): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961808 | |||||||
| chr5:156961808 | C | CAAAAA | 10 | a0001c0001t0001g0024 a0001c0001t0001g0228 a0001c0001t0001g0277 others(7): Show |
10 | HG01346.hp1 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.58+1328_58+1332dup others(5): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961808 | |||||||
| chr5:156961808 | CA | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0058 others(4): Show |
9 | HG01099.hp1 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+1332delT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961808 | |||||||
| chr5:156961808 | CAAA | C | 32 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0048 others(29): Show |
39 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.58+1330_58+1332del others(3): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961808 | |||||||
| chr5:156961808 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0057 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.58+1319_58+1332del others(14): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961808 | |||||||
| chr5:156961808 | CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02027.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.58+1318_58+1332del others(15): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961808 | |||||||
| chr5:156961808 | CAAAAAAA others(11): Show |
C | 5 | a0002c0003t0001g0045 a0002c0003t0001g0230 a0002c0003t0001g0231 others(2): Show |
5 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+1315_58+1332del others(18): Show |
TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961808 | |||||||
| chr5:156961819 | A | G | 1 | a0001c0008t0001g0229 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.58+1322T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961819 | |||||||
| chr5:156961822 | A | G | 32 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0048 others(29): Show |
39 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.58+1319T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961822 | |||||||
| chr5:156961833 | A | G | 1 | a0001c0008t0001g0229 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.58+1308T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961833 | |||||||
| chr5:156961837 | G | A | 2 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
2 | HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.58+1304C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961837 | |||||||
| chr5:156961841 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.58+1300C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961841 | |||||||
| chr5:156961841 | GA | G | 12 | a0001c0001t0001g0137 a0001c0001t0001g0281 a0001c0001t0001g0282 others(9): Show |
12 | HG01358.hp2 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.58+1299delT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961841 | |||||||
| chr5:156961848 | A | G | 15 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0002g0005 others(12): Show |
19 | HG01884.hp2 HG02451.hp2 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.58+1293T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961848 | |||||||
| chr5:156961849 | A | G | 1 | a0005c0006t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.58+1292T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156961849 | |||||||
| chr5:156962081 | G | A | 1 | a0001c0001t0003g0278 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.58+1060C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156962081 | |||||||
| chr5:156962143 | G | A | 1 | a0001c0008t0001g0229 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.58+998C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156962143 | |||||||
| chr5:156962224 | T | C | 4 | a0002c0003t0001g0230 a0002c0003t0001g0231 a0002c0003t0001g0232 others(1): Show |
4 | HG01070.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+917A>G | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156962224 | |||||||
| chr5:156962332 | TC | T | 6 | a0003c0004t0001g0004 a0003c0004t0001g0028 a0003c0004t0001g0029 others(3): Show |
7 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+808delG | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156962332 | |||||||
| chr5:156962408 | TA | T | 227 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(224): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.58+732delT | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156962408 | |||||||
| chr5:156962480 | G | A | 9 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(6): Show |
9 | HG02257.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.58+661C>T | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156962480 | |||||||
| chr5:156962552 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.58+589G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156962552 | |||||||
| chr5:156962571 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 |
3 | HG01081.hp1 HG01257.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.58+570G>A | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156962571 | |||||||
| chr5:156962612 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.58+529T>C | TIMD4 | ENSG00000145850.9 | transcript | ENST00000274532.7 | protein_coding | 1/8 | chr5 | 156962612 |